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Immunogenicity of standard and extended dosing intervals of BNT162b2 mRNA vaccine
Open accessAbstract
Extension of the interval between vaccine doses for the BNT162b2 mRNA vaccine was introduced in the United Kingdom to accelerate population coverage with a single dose. At this time, trial data were lacking, and we addressed this in a study of United Kingdom healthcare workers. The first vaccine dose induced protection from infection from the circulating alpha (B.1.1.7) variant over several weeks. In a substudy of 589 individuals, we show that this single dose induces severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) neutralizing antibody (NAb) responses and a sustained B and T cell response to the spike protein. NAb levels were higher after the extended dosing interval (6–14 weeks) compared with the conventional 3- to 4-week regimen, accompanied by enrichment of CD4 + T cells expressing interleukin-2 (IL-2). Prior SARS-CoV-2 infection amplified and accelerated the response. These data on dynamic cellular and humoral responses indicate that extension of the dosing interval is an effective immunogenic protocol.
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“Nonetheless, a growing number of studies suggest that an extended dosing interval amplifies both the humoral immune response30 and perhaps the cellular response,31 and is an effective global strategy given the discrepancies between regions with high and low vaccination coverage.32”
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Safety and Efficacy of the BNT162b2 mRNA Covid-19 Vaccine
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“Although Pfizer’s clinical trial described an efficacy of 52% against symptomatic infection after a single dose (Polack et al., 2020), the United Kingdom’s Joint Committee on Vaccination and Immunisation (JCVI) estimated an efficacy of 89% against symptomatic infection, having removed infection…”
BackgroundSelf-citationWhat level of neutralising antibody protects from COVID-19?
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Metadata
- Authors
- Payne, R. P., Longet, S., Austin, J. A., Skelly, D. T., Dejnirattisai, W., Adele, S., Meardon, N., Faustini, S., Al-Taei, S., Moore, S. C., Tipton, T., Hering, L. M., Angyal, A., Brown, R., Nicols, A. R., Gillson, N., Dobson, S. L., Amini, A., Supasa, P., Cross, A., Bridges-Webb, A., Reyes, L. S., Linder, A., Sandhar, G., Kilby, J. A., Tyerman, J. K., Altmann, T., Hornsby, H., Whitham, R., Phillips, E., Malone, T., Hargreaves, A., Shields, A., Saei, A., Foulkes, S., Stafford, L., Johnson, S., Wootton, D. G., Conlon, C. P., Jeffery, K., Matthews, P. C., Frater, J., Deeks, A. S., Pollard, A. J., Brown, A., Rowland-Jones, S. L., Mongkolsapaya, J., Barnes, E., Hopkins, S., Hall, V., Dold, C., Duncan, C. J. A., Richter, A., Carroll, M., Screaton, G., de Silva, T. I., Turtle, L., Klenerman, P., Dunachie, S., Abuelgasim, H., Adland, E., Adlou, S., Akther, H. D., Alhussni, A., Ali, M., Ansari, M. A., Arancibia-Cárcamo, C. V., Bayley, M., Brown, H., Chalk, J., Chand, M., Chawla, A., Chinnakannan, S., Cutteridge, J., de Lara, C., Denly, L., Diffey, B., Dimitriadis, S., Drake, T. M., Donnison, T., Dupont, M., Eyre, D., Fairman, A., Gardiner, S., Gilbert-Jarmillo, J., Goulder, P., Hackstein, C.-P., Hambleton, S., Haniffa, M., Haworth, J., Holmes, J., Horner, E., Jämsén, A., Johnson, S., Jones, C., Kasanyinga, M., Kelly, S., Kirk, R., Knight, M. L., Lawrie, A., Lee, L., Lett, L., Lillie, K., Lim, N., Mehta, H., Mentzer, A. J., O’Donnell, D., Ogbe, A., Pace, M., Payne, B. A. I., Platt, G., Poolan, S., Provine, N., Ramamurthy, N., Robinson, N., Romaniuk, L., Rongkard, P., Sampson, O. L., Simmons, B., Spegarova, J. S., Stephenson, E., Subramaniam, K., Thaventhiran, J., Thomas, S., Travis, S., Tucker, S., Turton, H., Watson, A., Watson, L., Weeks, E., Wilson, R., Wood, S., Wright, R., Xiao, H., & Zawia, A. A. T.
- Affiliations
- Newcastle University (GB)
- University of Liverpool (GB)
- University of Oxford (GB)
- Centre for Human Genetics (GB)
- Sheffield Teaching Hospitals NHS Foundation Trust (GB)
- University of Birmingham (GB)
- University of Sheffield (GB)
- Public Health England (GB)
- Liverpool University Hospitals NHS Foundation Trust (GB)
- Great North Children's Hospital (GB)
- University Hospitals Birmingham NHS Foundation Trust (GB)
- Oxford University Hospitals NHS Trust (GB)
- Siriraj Hospital (TH)
- Newcastle upon Tyne Hospitals NHS Foundation Trust (GB)
- Corresponding author
- Payne, Rebecca P.
- Klenerman, Paul
- ORCID
- Payne, Rebecca P.
- Austin, James A.
- Skelly, Donal T.
- Dejnirattisai, Wanwisa
- Adele, Sandra
- Faustini, Sian
- Moore, Shona C.
- Tipton, Tom
- Hering, Luisa M.
- Angyal, Adrienn
- Brown, Rebecca
- Nicols, Alexander R.
- Gillson, Natalie
- Dobson, Susan L.
- Amini, Ali
- Supasa, Piyada
- Reyes, Laura Silva
- Linder, Aline
- Tyerman, Jessica K.
- Altmann, Thomas
- Hornsby, Hailey
- Phillips, Eloise
- Hargreaves, Alexander
- Shields, Adrian
- Saei, Ayoub
- Foulkes, Sarah
- Stafford, Lizzie
- Conlon, Christopher P.
- Jeffery, Katie
- Matthews, Philippa C.
- Frater, John
- Deeks, Alexandra S.
- Pollard, Andrew J.
- Brown, Anthony
- Mongkolsapaya, Juthathip
- Barnes, Eleanor
- Hopkins, Susan
- Hall, Victoria
- Dold, Christina
- Duncan, Christopher J.A.
- Richter, Alex
- Carroll, Miles
- Screaton, Gavin
- de Silva, Thushan I.
- Turtle, Lance
- Klenerman, Paul
- Dunachie, Susanna
- Abuelgasim, Hibatullah
- Alhussni, Ahmed
- Ali, Mohammad
- Ansari, M. Azim
- Arancibia-Cárcamo, Carolina V.
- Chalk, Jeremy
- Chand, Meera
- Chinnakannan, Senthil
- Cutteridge, Joseph
- de Lara, Catherine
- Denly, Lucy
- Dimitriadis, Stavros
- Drake, Thomas M.
- Donnison, Timothy
- Dupont, Maeva
- Eyre, David
- Gardiner, Siobhan
- Goulder, Philip
- Hackstein, Carl-Philipp
- Hambleton, Sophie
- Haniffa, Muzlifah
- Holmes, Jennifer
- Horner, Emily
- Kasanyinga, Mwila
- Knight, Michael L.
- Lawrie, Allan
- Lee, Lian
- Lett, Lauren
- Lillie, Katy
- Lim, Nicholas
- Mentzer, Alexander J.
- Ogbe, Ane
- Pace, Matthew
- Payne, Brendan A.I.
- Platt, Gareth
- Provine, Nicholas
- Ramamurthy, Narayan
- Rongkard, Patpong
- Sampson, Oliver L.
- Spegarova, Jarmila S.
- Stephenson, Emily
- Thaventhiran, James
- Thomas, Sarah
- Travis, Simon
- Turton, Helena
- Watson, Adam
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2021-11
- Volume
- 184
- Issue
- 23
- Pages
- 5699-5714.e11
- ISSN
- 0092-8674 (ISSN-L)
- PMC
- PMC8519781
- OpenAlex
- W3206717788
- Cited by
- 322
- References
- 47
- Citations by year
- 2026: 14 · 2025: 33 · 2024: 34 · 2023: 87 · 2022: 135 · 2021: 18
- FWCI
- 21.70
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Cell (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (acceptedVersion)
- University of Birmingham Research Portal (University of Birmingham) (submittedVersion, cc-by)
- Greater South Information System
- Funders
- University of Liverpool
- Oxford University
- UK Research and Innovation
- Wellcome Trust (NIHR300791, 216417/Z/19/Z, 204721/Z/16/Z, 110058/Z/15/Z)
- U.S. Food and Drug Administration
- National Institute for Health Research
- Utah Department of Health
- Sheffield Teaching Hospitals NHS Foundation Trust
- Department of Health and Social Care
- University of Birmingham
- British Heart Foundation (FS/18/52/33808, PG/11/116/29288)
- Public Health England
- Topics
- Health Sciences › Medicine › Infectious Diseases › SARS-CoV-2 and COVID-19 Research
- Life Sciences › Immunology and Microbiology › Immunology › Immune responses and vaccinations
- Social Sciences › Health › Vaccine Coverage and Hesitancy
- Keywords
- BNT162b2 mRNA vaccine, extended dosing interval, single-dose vaccination, immunogenicity, neutralizing antibodies, spike protein, CD4+ T cells, interleukin-2, SARS-CoV-2, prior SARS-CoV-2 infection, healthcare workers
- MeSH terms
- COVID-19, SARS-CoV-2, COVID-19 Vaccines, mRNA Vaccines, BNT162 Vaccine, Adult, Aged, Antibodies, Viral, Dose-Response Relationship, Immunologic, Ethnicity, Female, Humans, Immunoglobulin G, Immunity, Male, Middle Aged, Reference Standards, T-Lymphocytes, Vaccines, Synthetic, Linear Models, Treatment Outcome, Cross-Priming, Young Adult, Antibodies, Neutralizing
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